MicroBlender R219P24-002

GUDID 00817770022374

Low Flow MicroBlender with Flowmeters (China Labeled)

MAXTEC, LLC

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• Primary Device ID: 00817770022374
• NIH Device Record Key: 58d6a97b-796a-4b0a-90ac-0b558a8d4692
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MicroBlender
• Version Model Number: Low Flow NIST
• Catalog Number: R219P24-002
• Company DUNS: 169911828
• Company Name: MAXTEC, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817770022374 [Primary]

FDA Product Code

• BZR: Mixer, Breathing Gases, Anesthesia Inhalation

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-16
• Device Publish Date: 2023-06-08

On-Brand Devices [MicroBlender]

• 00817770021629: High Flow with NIST Fitting
• 00817770020714: Low Flow
• 00817770022374: Low Flow MicroBlender with Flowmeters (China Labeled)